3904-16-3

Basic information

• Product Name: 1-Amino-1-phenylacetone hydrochloride
• Synonyms: 1-AMINO-1-PHENYLACETONE HYDROCHLORIDE;1-AMINO-1-PHENYLPROPAN-2-ONEHYDROCHLORIDE;1-Amino-1-phenylacetone hydrochloride, 2-Oxo-1-phenylpropylamine hydrochloride
• CAS NO: 3904-16-3
• Molecular Formula: C₉H₁₁NO*ClH
• Molecular Weight: 185.65
• Product Categories: Phenyls & Phenyl-Het;Phenyls & Phenyl-Het
• Mol File: 3904-16-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 235.2 °C at 760 mmHg
• Flash Point: 96.1 °C
• Appearance: /
• Vapor Pressure: 0.0506mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 1-Amino-1-phenylacetone hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Amino-1-phenylacetone hydrochloride(3904-16-3)
• EPA Substance Registry System: 1-Amino-1-phenylacetone hydrochloride(3904-16-3)

Safety Data

• Hazardous Substances Data: 3904-16-3(Hazardous Substances Data)

Usage

General Description

1-Amino-1-phenylacetone hydrochloride is a chemical compound with the molecular formula C8H11NO?HCl. It is commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds. 1-Amino-1-phenylacetone hydrochloride is a white to off-white crystalline powder that is soluble in water, alcohol, and chloroform. It is also known by the trade name P2NP HCl and is classified as a controlled substance due to its potential for misuse and abuse. It is important to handle and use this chemical with care and in accordance with all applicable laws and regulations.

InChI:InChI=1/C9H11NO.ClH/c1-7(11)9(10)8-5-3-2-4-6-8;/h2-6,9H,10H2,1H3;1H

Upstream product

• 25355-34-4 1-phenyl-propane-1,2-dione 1-oxime 
• 103-01-5 N-Phenylglycine 
• 103-79-7 1-phenyl-acetone 

Downstream Products

• 54600-85-0 2,5-dimethyl-3,6-diphenylpyrazine 
• 107324-97-0 3-(4-Nitro-phenoxy)-N-(2-oxo-1-phenyl-propyl)-propionamide 
• 52500-61-5 2-hydroxy-1-phenylpropylamine 
• 1439370-60-1 7-(dimethylamino)-3-methyl-2-phenylchromeno[4,3-b]pyrrol-4(1H)-one 
• 1439370-58-7 4-((2-oxo-1-phenylpropyl)amino)-3-acetyl-7-dimethylaminocoumarin 
• 1439370-56-5 4-((2-oxo-1-phenylpropyl)amino)-3-benzoyl-7-dimethylaminocoumarin 
• 107325-11-1 sodium salt of 5-{4-[2-(5-methyl-4-phenyl-2-oxazolyl)ethoxy]benzyl}-2,4-thiazolidinedione 
• 107324-92-5 2-imino-5-{4-[2-(5-methyl-4-phenyl-2-oxazolyl)ethoxy]benzyl}-4-thiazolidinone 
• 107325-04-2 5-Methyl-2-[2-(4-nitro-phenoxy)-ethyl]-4-phenyl-oxazole 
• 141399-51-1 4-[2-(5-Methyl-4-phenyl-oxazol-2-yl)-ethoxy]-phenylamine 
• 88122-90-1 (+/-)-5c-methyl-2,4r-diphenyl-4,5-dihydro-oxazole 
• 88122-90-1 trans-5-methyl-2,4-diphenyl-Δ²-oxazoline 
• 131003-73-1 4-Methyl-N-(2-oxo-1-phenyl-propyl)-benzamide 
• 92962-80-6 N-(2-oxo-1-phenylpropyl)benzamide 

Relevant articles and documents

Synthesis of coumarin/pyrrole-fused heterocycles and their photochemical and redox-switching properties

Two coumarin/pyrrole-fused heterocycles were synthesized to investigate their photochemical and redox-switching properties. Photooxidation of the colorless diphenyl-substituted pyrrolocoumarin resulted in a distinct change to red and a sharp decrease in f

ISOQUINOLINE SYNTHESIS VIA 2-OXAZOLINES. PART VI. TRANSFORMATION OF 1-BENZAMIDO-1-PHENYL-2-ALKANOLS INTO 4-ALKYL-1-PHENYLISOQUINOLINES

Conditions necessary for the transformation of 1-benzamido-1-phenyl-2-alkanols (1) and 5-alkyl-2,4-diphenyl-2-oxazolines (2) into 4-alkyl-1-phenylisoquinolines (3) have been determined.The mechanism proposed for these reactions is supported by the results